[Selective progesterone receptor modulator (ulipristal acetate--a new option in
the pharmacological treatment of uterine fibroids in women]. [Article in Polish]
Author(s): Szamatowicz M(1), Kotarski J.
Affiliation(s): Author information:
(1)Klinika Ginekologii i Onkologii Ginekologicznej UM w BiaĆymstoku, Polska.
szamatow@umb.edu.pl
Publication date & source: 2013, Ginekol Pol. , 84(3):219-22
Uterine leiomyomata (fibroids) are very common, mostly benign tumors in women of
reproductive age. Symptomatic fibroids cause significant morbidity and are
characterized by heavy prolonged menstrual bleeding, by pain and pelvic pressure
and, in some cases, they may lead to reproductive dysfunctions. Up to date,
surgical procedures (hysterectomy or myomectomy) have been the dominant
managements but recently uterine artery embolization and focused ultrasound
surgery have also been taken into consideration. Hysterectomy is curative but for
women of reproductive age the need for uterus-sparing medical therapy is evident.
There are convincing data that progesterone and its receptors increase the
proliferation activity of the cells in uterine leiomyomata, hence treatment with
antiprogestins and progesterone receptor modulators seems to be reasonable.
Results of a successfully completed phase III clinical trials with the
application of ulipristal acetate (UPA) (first-in-class selective progesterone
receptor modulator--SPRM) have been published at the beginning of this year
Administration of 5 mg or 10 mg UPA daily has been shown to rapidly stop (within
a week) excessive uterine bleeding, reduce the volume of the three largest
fibroids by -44.8% and -54.8% for UPA 5 mg and 10 mg, respectively The effect on
fibroid volume has been observed for up to 6 months after treatment cessation. It
is also important that UPA restores patient Quality of Life scores to the level
of healthy women and in the majority of patients resumes menstruation and
ovulation within one month after treatment cessation. When compared with the
Gn-RH agonist (leuprolide acetate), UPA has controlled uterine bleeding faster
and more consistently (7 days vs. 30 days), fibroid reduction for up to 6 months
has been smaller for Gn-RH a (-16.5%) and UPA has shown a superior safety profile
as estradiol levels are maintained in the mid-follicular range. The UPA has
caused temporary changes in endometrial morphology but 6 month after the
treatment the endometrium returned to normal histology in the majority of cases.
The presented results on the application UPA in the medical treatment of
symptomatic uterine fibroids are very promising and gynecologists are given a new
treatment option.
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